Loh E Y, Elliott J F, Cwirla S, Lanier L L, Davis M M
Departments of Medicine and Microbiology and Immunology, Stanford University School of Medicine, CA 94305-5402.
Science. 1989 Jan 13;243(4888):217-20. doi: 10.1126/science.2463672.
In the polymerase chain reaction (PCR), two specific oligonucleotide primers are used to amplify the sequences between them. However, this technique is not suitable for amplifying genes that encode molecules where the 5' portion of the sequences of interest is not known, such as the T cell receptor (TCR) or immunoglobulins. Because of this limitation, a novel technique, anchored polymerase chain reaction (A-PCR), was devised that requires sequence specificity only on the 3' end of the target fragment. It was used to analyze TCR delta chain mRNA's from human peripheral blood gamma delta T cells. Most of these cells had a V delta gene segment not previously described (V delta 3), and the delta chain junctional sequences formed a discrete subpopulation compared with those previously reported.
在聚合酶链反应(PCR)中,使用两个特定的寡核苷酸引物来扩增它们之间的序列。然而,该技术不适用于扩增编码分子的基因,这些分子的感兴趣序列的5'部分未知,例如T细胞受体(TCR)或免疫球蛋白。由于这一局限性,人们设计了一种新技术——锚定聚合酶链反应(A-PCR),该技术仅要求在靶片段的3'端具有序列特异性。它被用于分析来自人外周血γδT细胞的TCRδ链mRNA。这些细胞中的大多数具有先前未描述的Vδ基因片段(Vδ3),并且与先前报道的相比,δ链连接序列形成了一个离散的亚群。